UMD-MEN1 database: an overview of the 370 MEN1 variants present in 1,676 patients from the French population.

Fiche publication

Date publication

octobre 2018


The Journal of clinical endocrinology and metabolism


Membres identifiés du Cancéropôle Est :
Dr GOUDET Pierre

Tous les auteurs :
Romanet P, Mohamed A, Giraud S, Odou MF, North MO, Pertuit M, Pasmant E, Coppin L, Guien C, Calender A, Borson-Chazot F, Béroud C, Goudet P, Barlier A


Multiple Endocrine Neoplasia type 1 (MEN1) is an autosomal dominant disease caused by mutations in the MEN1 gene characterized by a broad spectrum of clinical manifestations, of which the most frequent are primary hyperparathyroidism, pituitary adenomas, and neuroendocrine tumors.


J. Clin. Endocrinol. Metab.. 2018 Oct 18;: